Effects of transcutaneous electrical stimulation on peripheral nerve regeneration after digital neurorrhaphy: A randomized clinical trial.

Introduction

The human hand is a rich sensory and motor multifunctional tool with dexterous control to perform essential manipulation tasks.¹ Peripheral nerve injuries, especially of the upper limb, can result in severe disability and reduced quality of life.^2–4 Several strategies^5–8 including the use of neurotrophic factors, stem cell therapy,^9,10 and electrical stimulation,¹¹ have been investigated to promote peripheral nerve regeneration as well as functional recovery after these traumas.¹² Electrical stimulation has also been considered as an ancillary to surgical repair, and its effects on nerve recovery has been the focus of several studies.^13–25

It is to be noted that the characteristics and regenerative potential of peripheral nerves differ markedly depending on the location and type of lesion.²⁶ Differences in digital nerve lesions compared with more proximal and mixed lesions are described.^26,27 Digital nerves are almost exclusively sensory, and injuries to these nerves, properly repaired, generally have shorter regeneration distances and can serve as a model for evaluating the effects of transcutaneous peripheral electrical stimulation (PES), delivered through surface electrodes (commonly referred to as TENS).²⁷ By contrast, proximal nerve injuries, or nerve injuries with larger gaps to overcome, may be more difficult to completely regenerate, given the increased length for axonal growth and the complexity of motor and sensory functional recovery.²⁸

There are different ways to deliver the PES such as implanted electrodes,^15,16 percutaneous electrostimulation^17,18 (acupuncture needles inserted into the skin and connected to an electric current generator), intraoperative electrostimulation,^19–23 thin-film wireless implantable nerve stimulators,²⁴ and surface electrodes.²⁵ The use of transcutaneous surface electrodes is a non-invasive, practical, and simple option, avoiding the reactions provoked by implant surgery or percutaneous stimulation.²⁹

Based on these considerations, we hypothesized that a brief, early postoperative session of transcutaneous PES could modulate biological mechanisms associated with nerve regeneration following digital neurorrhaphy. This hypothesis was grounded on evidence from experimental and clinical studies showing that short-duration electrical stimulation applied soon after nerve repair may enhance activity-dependent regenerative processes.^23,30 In the present study, we intentionally adapted these principles to a non-invasive and clinically feasible protocol, consisting of a single 1-hour session of surface stimulation delivered at motor threshold within 24 hours after surgery. The stimulation protocol (20 Hz, 1 hour) was selected based on the findings of Al-Majed et al. (2000),¹⁹ which identified this window as optimal for the upregulation of BDNF and TrkB mRNA. Although the digital nerve is sensory, the intensity was calibrated to the motor threshold of the median nerve to ensuring supramaximal recruitment of large-diameter A-beta sensory fibers, which share similar electrical thresholds with A-alpha motor fibers. Although this approach aimed to reproduce, in a transcutaneous manner, stimulation parameters previously associated with regenerative benefits, its biological effectiveness in purely sensory digital nerves remains unclear. Therefore, we conducted a randomized clinical trial to investigate whether this specific surface PES protocol could influence sensory recovery, cold sensitivity, and pain-related disability in patients undergoing digital nerve repair.

Methods

This double-blind, randomized, controlled clinical trial was conducted at a general hospital in Bahia, Brazil, from December 19, 2020, to June 10, 2022. The study was prospectively registered in the Brazilian Clinical Trials Registry (ReBEC) on December 18, 2020 (registration number: U1111-1259-1998; available at: https://ensaiosclinicos.gov.br/rg/RBR-8xn3qq5). Ethical approval was obtained from the Research Ethics Committee of the Faculty of Medicine of Bahia, and the study protocol was published³¹ in advance to ensure methodological transparency and compliance with the Declaration of Helsinki.³²

Interventions

All patients underwent standardized microsurgical neurorrhaphy under ultrasound-guided axillary block, with epineural approximation using 2 to 4 nylon 8-0 sutures to align nerve fascicles and minimize trauma. Within 24 hours after surgery, participants were randomly allocated to one of two groups.

The stimulation parameters were chosen based on previous studies related to nerve regeneration and patient safety.^11,14,15,19 Group A (Surgery + PES) received one hour of transcutaneous electrical stimulation using the Neurodyn II device (Ibramed, Brazil), delivering a square-pulsed, biphasic, symmetrical current at 20 Hz with a 0.4 ms pulse width, at the motor threshold of the median nerve. Group B (Surgery + sham PES) underwent an identical setup with the same device and electrode positioning, but after an initial perceptible activation, the device output was reduced to zero for the remainder of the session. In both groups, two 1 x1 cm silicone-carbon gel electrodes were positioned proximally and distally to the surgical site ensuring identical placement to maintain blinding of both participants and the administering physiotherapist ( Figure 2). A certified physiotherapist, blinded to the group allocation, supervised the rehabilitation protocol. Sessions were remotely monitored via electronic platforms such as WhatsApp or Skype. Patients underwent a hand sensory re-education program based on the approach proposed by Dellon & Jabaley (1982),³³ focused on hand sensory re-education over 3-month period. Participants were also encouraged to perform complementary exercises in a home-based program.

Figure 1. CONSORT 2010 flowchart diagram of patient screening, intervention, and follow-up.

*Intention-to-treat (ITT) analysis.

Figure 2. Model of a repaired digital nerve injury of the index finger and the electrodes placement.

Results

Eligibility was evaluated in a total of 54 patients. Of these, 21 did not meet the inclusion criteria, and one declined to participate. Thus, 32 patients were randomized, with 16 allocated to the PES group and 16 to the sham group ( Figure 1). Baseline characteristics were comparable between groups, and all participants presented with severe sensory impairment on preoperative evaluation, assessed by MSW and s2PD tests ( Table 1). No significant differences between groups were observed during the immediate postoperative period (up to one week; p > 0.05), so subsequent statistical analyses focused on the 1- and 3-month follow-up data.

Sensory outcomes improved over time in both groups, with significant changes observed between 1 and 3 months postoperatively. Repeated measures ANOVA demonstrated a significant effect of time for both SWM (p = 0.012) and s2PD (p = 0.002), indicating progressive sensory recovery in both groups. No significant group effect or group–time interaction was observed for either outcome (p > 0.05). Age showed a marginal influence on SWM outcomes (p = 0.082), becoming significant when scores were converted to needle size (p = 0.014) ( Figure 3).

Figure 3. Sensory and patient-reported outcomes after digital nerve repair in the PES and sham groups.

Top panels show mean Semmes-Weinstein monofilament thresholds (SWM, grams) and static two-point discrimination (s2PD, millimeters) at 1 and 3 months postoperatively. Both groups demonstrated progressive sensory recovery over time, with no significant differences between PES and sham. Bottom panels show Cold Sensitivity Severity Scale (CSS) and Pain Disability Index (PDI, 0–70) scores at 3 months. Error bars represent standard error of the mean.

As CSS and PDI were assessed only at the 3-month follow-up, comparisons between groups were performed using an independent samples t-test at this single time point. No statistically significant differences were found. However, the two scales were highly correlated (r = 0.819, p < 0.001), suggesting consistent subjective perception of disability and cold sensitivity among patients. Age was initially included as a covariate due to its known influence on nerve regeneration. To assess the robustness of the results, sensitivity analyses were performed by (1) excluding age as a covariate and (2) removing an outlier, a 57-year-old participant from the PES group with discrepant SWM values (z-score ≈ 5).

In summary, the results show that patients from both groups recovered gradually their sensitivity as measured by MSW and s2PD tests, reaching a satisfactory level at the last measurement. However, no significant treatment effect was found across time points, with overlapping confidence intervals and small effect sizes between groups, as shown in Figure 3. Importantly, these sensitivity analyses did not alter the primary conclusions of the study.

Discussion

This randomized controlled trial investigated the effectiveness of surface PES in promoting sensory recovery following digital nerve neurorrhaphy. Both groups exhibited a gradual recovery of sensory function over the 3-month follow-up, as measured by SWM and s2PD tests. From a theoretical perspective, electrical stimulation is thought to enhance nerve regeneration through activity-dependent mechanisms that require effective recruitment of regenerating axons and sufficient current density at the nerve site. In the present study, the transcutaneous delivery of stimulation, applied at motor threshold in a purely sensory nerve injury, may not have provided the selectivity or intensity of fiber activation necessary to trigger these mechanisms.⁴¹ Although age showed a near-significant effect in some models, its overall influence appears limited. Cold sensitivity and pain-related disability were assessed only at the final follow-up and showed high inter-individual variability, limiting the ability to draw definitive conclusions regarding these secondary outcomes. Transcutaneous electrical stimulation holds promise in nerve regeneration, offering a non-invasive approach with potential practical benefits.⁴² It can be utilized to circumvent the complications of surgical implantation or percutaneous stimulation.^43,44

Some research indicates that it may take up to 8 weeks for the regenerating axons to cover a distance of 25mm, and the use of PES may reduce this period.^20,26 Previous results demonstrated that subjects who received stimulation exhibited earlier and better outcomes around 3 months post-surgery.²⁶ Gordon at al. (2010)²³ conducted an innovative randomized controlled trial (RCT) of 21 patients undergoing carpal tunnel decompression surgery. Postoperative direct nerve stimulation using implanted wires (20 Hz, 4-6 volts 0.1-0.8 ms) for one hour led to earlier improvements in electrophysiological parameters when compared to controls. Simillarly, Wong et al. (2015)²⁶ conducted a double-blind RCT involving 31 patients with transected digital nerves and observed significantly improved sensory outcomes with PES (20 Hz, <30 V, 0.1–0.4 ms), although no differences in overall functional recovery were found. In another trial, Power et al. (2020)⁴⁵ evaluated PES following cubital tunnel decompression in 31 patients. The intervention group received a single 1-hour session of PES (20 Hz, <30 V, 0.1 ms) and demonstrated greater improvements in Motor Unit Number Estimation (MUNE) over time compared to the control group. Importantly, these studies employed direct, implanted, or intraoperative stimulation, ensuring higher current density and selective activation of nerve fibers at the repair site, conditions that differ substantially from transcutaneous stimulation and may explain the discrepancy in findings.

Some studies reported adverse findings that contradict prior research that has highlighted the advantageous impact of direct current electric fields on the regeneration of peripheral nerves.^46,47 In the present trial, neither the s2PD nor the SWM tests demonstrated a significant enhancement in tactile receptor reinnervation in the digital pulp among patients who received PES. Given these results, the effectiveness of transcutaneous applied electrical fields in promoting in vivo peripheral nerve regeneration remains uncertain.

Cold intolerance⁴⁸ and pain⁴⁹ are commonly reported sources of substantial morbidity following nerve injuries in the hand. Previous studies have associated the severity of these symptoms with the degree of sensory recovery, with poorer reinnervation correlating with more pronounced functional impairment and discomfort.^49,50 In the present sample, isolated digital nerve injuries were not associated with worse outcomes in terms of pain or cold intolerance, as measured by the CSS and PDI. These symptoms appear to be more commonly linked to complex cases involving finger replantation, severe vascular compromise, or proximal nerve injuries of the median or ulnar nerves.

Postoperative rehabilitation following hand neurorrhaphy is considered standard of care⁵¹ and was prescribed for all participants in this study. Withholding rehabilitation would be ethically inappropriate, as hand therapy is routinely recommended after surgery in real-world clinical settings. Omission of such care could also compromise the study’s external validity. Nevertheless, it is important to acknowledge the potential for interaction effects between the rehabilitation protocol and the electrical stimulation intervention,⁵² which may have limited the ability to isolate the specific contribution of PES to sensory recovery.

The use of a digital nerve injury model in this study presents inherent limitations regarding the generalizability of the findings. Digital nerve injuries differ substantially from proximal or mixed nerve lesions, particularly due to the shorter axonal regeneration distances and the absence of motor components. Because isolated digital nerve injuries typically show rapid and favorable recovery after repair, the short regeneration distance may have produced a ceiling effect by three months, limiting the ability of standard measures such as SWM and s2PD to detect small incremental differences between groups.^53–55 Consequently, although our findings provide insight into the effects of PES on sensory nerve regeneration in the hand, they may not be directly applicable to more severe or complex nerve injuries requiring longer regenerative distances. Future studies should consider the use of more complex clinical models, such as proximal or mixed nerve injuries, to better assess the potential of electrical stimulation in promoting meaningful functional recovery. Therefore, the present findings should be interpreted as evidence regarding the limitations of this specific stimulation paradigm in this clinical model, rather than as evidence against the potential usefulness of electrical stimulation as a broader therapeutic strategy for peripheral nerve regeneration.

Conclusion

The specific protocol of surface PES tested in this study may not confer additional clinical benefit in isolated digital nerve injuries under standard rehabilitation conditions. No significant differences were observed in cold sensitivity or pain-related disability outcomes between the intervention and control groups. These findings suggest that, within the context of isolated digital nerve injuries, surface PES may not confer additional clinical benefit beyond standard surgical repair and rehabilitation. Further research is warranted to explore the efficacy and safety of electrical stimulation protocols in more complex nerve injury models and under varying clinical conditions.

Ethical considerations

This study was approved by the Research Ethics Committee of the Faculty of Medicine of Bahia (Federal University of Bahia), under protocol number 4.430.230. All procedures were conducted in accordance with the Declaration of Helsinki. The study was prospectively registered in the Brazilian Clinical Trials Registry (ReBEC) under registration number U1111-1259-1998.

Consent to participate

All participants provided written informed consent prior to enrollment in the study, including consent for surgical intervention, application of surface PES, and participation in follow-up assessments.